A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6983096



Internal ID12974832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:18908268..18961087hg38UCSC Ensembl
Innerchr11:18929815..18982634hg19UCSC Ensembl
Innerchr11:18886391..18939210hg18UCSC Ensembl
Innerchr11:18886391..18939210hg17UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3852820
hg1952820
hg1852820
hg1752820
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2750991
Supporting Variants
SamplesBEC_543
Known GenesMRGPRX1
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6983096
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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